LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

Zabetian, Cyrus P

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. [electronic resource] - American journal of human genetics Oct 2006 - 752-8 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.

0002-9297

10.1086/508025 doi


Africa, Northern
Amino Acid Substitution
Case-Control Studies
Family
Female
Haplotypes
Humans
Jews--genetics
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Male
Middle East
Parkinson Disease--genetics
Polymorphism, Single Nucleotide
Protein Serine-Threonine Kinases--genetics
Software
White People--genetics